Cardiomyopathy Trial, Recruiting NCT07077005 Sponsor: Technical University of Munich Condition: Cardiomyopathy
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Cardiomyopathy Trial, Recruiting

NCT07077005
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • You must be 18 years of age or older
  • You must have been diagnosed with a heart condition called hypertrophic obstructive cardiomyopathy (a thickening of the heart muscle that blocks blood flow)
  • You must have been taking the same dose of a medication called mavacamten for at least 12 weeks without any changes
  • Your heart's blood flow measurements must be at or below a certain level, both at rest and during a stress test using ultrasound (confirm with trial site)
  • Your heart must be pumping at least 50% of its normal capacity at the time you join the study
  • Your heart symptoms must be mild — rated as Class I or II on a standard heart symptom scale, meaning you have little to no limitation during everyday activities

Who may not be able to join:

  • You have fainted or had a serious fast heart rhythm problem in the 6 months before joining the study
  • Your heart's electrical activity shows a reading that is too prolonged on a heart tracing test (confirm with trial site)
  • You have a type of irregular heartbeat called atrial fibrillation that comes and goes, shown on a heart tracing test at screening
  • You have a constant or long-term irregular heartbeat and have not been taking blood-thinning medication for at least 4 weeks
  • You have previously had a procedure or surgery to reduce the thickness of your heart muscle
  • During an exercise breathing test, you show signs of dangerous heart rhythm problems or concerning changes in your heart tracing
  • You have significant leaking or narrowing of one or more heart valves, seen on an ultrasound of your heart at rest
  • You already have an implanted heart device designed to correct dangerous heart rhythms (a defibrillator)
  • Your personal risk score for sudden cardiac death is calculated at 4% or higher (confirm with trial site)

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 12 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: 00498941406774

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Technical University of Munich
Registry
ClinicalTrials.gov
Start date
1 November 2025
Est. completion
31 October 2026

Where this trial is recruiting

🇩🇪 Germany

Primary endpoints

Incidence of Treatment-Emergent Adverse Events

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 12 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov